It starts with knowledge. We employ the best minds in the business—nearly
4,000 of them—all applying their extensive industry-based scientific and regulatory
expertise to your research. All working together to smooth the pathway to market for
your compound.
It continues with a global infrastructure of facilities strategically
located around the world, linked to a robust, integrated IT
network with superior reliability. MDS Pharma Services applies its advanced scientific
and technological expertise throughout the drug discovery and development process – from
lead optimization, pre-IND research, early clinical research (bioequivalence, phases I-IIa)
and bioanalysis through to global clinical development (phases II-IV), central lab and
centralized cardiac services.
It all comes together via an interconnected network of dedicated teams
focused on managing your projects through the drug development continuum. More
importantly, our capability and expertise to both customize and execute your research
and development programs further accelerate your drug's development.
MDS Pharma Services has created a Drug Development Programs service that
tailors our program management approach to meet the specific needs of each client,
providing full program and scientific consulting, project management and program
facilitation. Our Small Molecule Development Program is just one example of the
versatility and scope available through Development and Regulatory Services.
From the start, MDS Pharma Services works with you as an integrated team.
Our efforts are led by a senior level scientist/manager experienced in drug
development who serves as the program leader. All aspects, including contracting,
conduct and follow-up, are addressed through Development and Regulatory Services.
